ReP USP - Resultado da busca

Trabalho de evento-resumo
LH receptor mutations (2004)
Mendonca, B. B.; Arnhold, I. J.; Latronico, A. C.; Mendonca, B. B.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: RECEPTORES CELULARES, RECEPTORES DO FSH, RECEPTORES HORMONAIS, MUTAÇÃO GENÉTICA, GENES SUPRESSORES DE TUMOR
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ABNT
MENDONCA, B. B. et al. LH receptor mutations. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 06 nov. 2025.
APA
Mendonca, B. B., Arnhold, I. J., Latronico, A. C., & Mendonca, B. B. (2004). LH receptor mutations. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Mendonca BB, Arnhold IJ, Latronico AC, Mendonca BB. LH receptor mutations. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Vancouver
Mendonca BB, Arnhold IJ, Latronico AC, Mendonca BB. LH receptor mutations. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Effect of severe long-standing hyperandrogenemia on pituitary-gonadal axis in females with virilizing tumors (2004)
Ferraz de Souza, B.; D' Alva, C. B.; Normando, A. P. C.; Hayashida, S.; Mendonca, B. B.; Marcondes, J. A. M.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: NEOPLASIAS OVARIANAS (ETIOLOGIA;CIRURGIA), HORMÔNIOS HIPOTALÂMICOS (ANÁLISE), HORMÔNIOS SEXUAIS (DEFICIÊNCIA;ANORMALIDADES)
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ABNT
FERRAZ DE SOUZA, B. et al. Effect of severe long-standing hyperandrogenemia on pituitary-gonadal axis in females with virilizing tumors. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 06 nov. 2025.
APA
Ferraz de Souza, B., D' Alva, C. B., Normando, A. P. C., Hayashida, S., Mendonca, B. B., & Marcondes, J. A. M. (2004). Effect of severe long-standing hyperandrogenemia on pituitary-gonadal axis in females with virilizing tumors. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Ferraz de Souza B, D' Alva CB, Normando APC, Hayashida S, Mendonca BB, Marcondes JAM. Effect of severe long-standing hyperandrogenemia on pituitary-gonadal axis in females with virilizing tumors. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Vancouver
Ferraz de Souza B, D' Alva CB, Normando APC, Hayashida S, Mendonca BB, Marcondes JAM. Effect of severe long-standing hyperandrogenemia on pituitary-gonadal axis in females with virilizing tumors. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Mutational analysis of neuropeptide y-y1 receptor gene (npy-y1) in human idiopathic pubertal disorders (2004)
Freitas, K.; Brito, V.; Costa, E.; Arnhold, I.; Mendonca, B. B.; Latronico, A. C.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: HORMÔNIO DO CRESCIMENTO (SECREÇÃO), PUBERDADE PRECOCE (ANORMALIDADES;GENÉTICAS), SEQUENCIAMENTO GENÉTICO, HORMÔNIOS SEXUAIS (GENÉTICA)
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ABNT
FREITAS, K. et al. Mutational analysis of neuropeptide y-y1 receptor gene (npy-y1) in human idiopathic pubertal disorders. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 06 nov. 2025.
APA
Freitas, K., Brito, V., Costa, E., Arnhold, I., Mendonca, B. B., & Latronico, A. C. (2004). Mutational analysis of neuropeptide y-y1 receptor gene (npy-y1) in human idiopathic pubertal disorders. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Freitas K, Brito V, Costa E, Arnhold I, Mendonca BB, Latronico AC. Mutational analysis of neuropeptide y-y1 receptor gene (npy-y1) in human idiopathic pubertal disorders. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Vancouver
Freitas K, Brito V, Costa E, Arnhold I, Mendonca BB, Latronico AC. Mutational analysis of neuropeptide y-y1 receptor gene (npy-y1) in human idiopathic pubertal disorders. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
A novel mutation in the AVP-NPII gene in a Brazilian kindred with autossomal dominant neurohypophysed diabetes insipidus (2004)
Melo, M. E.; Marui, S.; Mendonca, B. B.; Knoepfelmacher, M.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: GENÓTIPOS (ANORMALIDADES), DIABETES INSÍPIDO (GENÉTICA), BRASILEIROS (GENÉTICA, SEQUENCIAMENTO GENÉTICO
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ABNT
MELO, M. E. et al. A novel mutation in the AVP-NPII gene in a Brazilian kindred with autossomal dominant neurohypophysed diabetes insipidus. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 06 nov. 2025.
APA
Melo, M. E., Marui, S., Mendonca, B. B., & Knoepfelmacher, M. (2004). A novel mutation in the AVP-NPII gene in a Brazilian kindred with autossomal dominant neurohypophysed diabetes insipidus. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Melo ME, Marui S, Mendonca BB, Knoepfelmacher M. A novel mutation in the AVP-NPII gene in a Brazilian kindred with autossomal dominant neurohypophysed diabetes insipidus. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Vancouver
Melo ME, Marui S, Mendonca BB, Knoepfelmacher M. A novel mutation in the AVP-NPII gene in a Brazilian kindred with autossomal dominant neurohypophysed diabetes insipidus. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Virilizing Leydig-cell ovarian tumor responsive to depot GnRH analoque (2004)
Ferraz de Souza, B.; Marcondes, J. A. M.; Mendonca, B. B.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: GONADOTROFINAS, HORMÔNIOS SEXUAIS FEMININOS (ANORMALIDADES), ANDRÓGENOS (ANORMALIDADES), NEOPLASIAS OVARIANAS (GENÉTICA;CIRURGIA;FISIOPATOLOGIA)
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ABNT
FERRAZ DE SOUZA, B. e MARCONDES, J. A. M. e MENDONCA, B. B. Virilizing Leydig-cell ovarian tumor responsive to depot GnRH analoque. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 06 nov. 2025.
APA
Ferraz de Souza, B., Marcondes, J. A. M., & Mendonca, B. B. (2004). Virilizing Leydig-cell ovarian tumor responsive to depot GnRH analoque. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Ferraz de Souza B, Marcondes JAM, Mendonca BB. Virilizing Leydig-cell ovarian tumor responsive to depot GnRH analoque. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Vancouver
Ferraz de Souza B, Marcondes JAM, Mendonca BB. Virilizing Leydig-cell ovarian tumor responsive to depot GnRH analoque. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
High frequency of allelic variants in SF-1 (Steroidogenic Factor 1) gene in 46,XY sex-reversed patients (2004)
Correa, R. V.; Domenice, S.; Billerberck, A. E. C.; Mendonca, B. B.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: ANORMALIDADES CROMOSSÔMICAS, AGENESIA, GÔNADAS ANIMAL (ANORMALIDADES), MUTAÇÃO GENÉTICA, CROMOSSOMOS (ANORMALIDADES)
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ABNT
CORREA, R. V. et al. High frequency of allelic variants in SF-1 (Steroidogenic Factor 1) gene in 46,XY sex-reversed patients. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 06 nov. 2025.
APA
Correa, R. V., Domenice, S., Billerberck, A. E. C., & Mendonca, B. B. (2004). High frequency of allelic variants in SF-1 (Steroidogenic Factor 1) gene in 46,XY sex-reversed patients. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Correa RV, Domenice S, Billerberck AEC, Mendonca BB. High frequency of allelic variants in SF-1 (Steroidogenic Factor 1) gene in 46,XY sex-reversed patients. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Vancouver
Correa RV, Domenice S, Billerberck AEC, Mendonca BB. High frequency of allelic variants in SF-1 (Steroidogenic Factor 1) gene in 46,XY sex-reversed patients. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Mutational analysis of the gaba-a receptor alpha1 subunit gene (gabra 1) in girls familial and sporadic idiophatic gonadotrpin-dependent precocious puberty (2004)
Brito, V.; Mendonca, B. B.; Freitas, k.; Arnhold, I.; Latronico, A. C.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: HORMÔNIO DO CRESCIMENTO (FISIOPATOLOGIA), PUBERDADE PRECOCE, POLIMORFISMO, GENES SUPRESSORES DE TUMOR (METABOLISMO), GONADOTROFINAS
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ABNT
BRITO, V. et al. Mutational analysis of the gaba-a receptor alpha1 subunit gene (gabra 1) in girls familial and sporadic idiophatic gonadotrpin-dependent precocious puberty. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 06 nov. 2025.
APA
Brito, V., Mendonca, B. B., Freitas, k., Arnhold, I., & Latronico, A. C. (2004). Mutational analysis of the gaba-a receptor alpha1 subunit gene (gabra 1) in girls familial and sporadic idiophatic gonadotrpin-dependent precocious puberty. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Brito V, Mendonca BB, Freitas k., Arnhold I, Latronico AC. Mutational analysis of the gaba-a receptor alpha1 subunit gene (gabra 1) in girls familial and sporadic idiophatic gonadotrpin-dependent precocious puberty. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Vancouver
Brito V, Mendonca BB, Freitas k., Arnhold I, Latronico AC. Mutational analysis of the gaba-a receptor alpha1 subunit gene (gabra 1) in girls familial and sporadic idiophatic gonadotrpin-dependent precocious puberty. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
The unusually high incidence of germline Arg337His mutation in the p53 tumor suppressor gene among brazilian with adrenocortical tumors can be attributed to founder effect (2004)
Pinto, E. M.; Billerbeck, A. E.; Mendonca, B. B.; Latronico, A. C.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: BIOMARCADORES, MUTAÇÃO GENÉTICA, POLIMORFISMO, GENES SUPRESSORES DE TUMOR, BRASILEIROS
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ABNT
PINTO, E. M. et al. The unusually high incidence of germline Arg337His mutation in the p53 tumor suppressor gene among brazilian with adrenocortical tumors can be attributed to founder effect. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 06 nov. 2025.
APA
Pinto, E. M., Billerbeck, A. E., Mendonca, B. B., & Latronico, A. C. (2004). The unusually high incidence of germline Arg337His mutation in the p53 tumor suppressor gene among brazilian with adrenocortical tumors can be attributed to founder effect. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Pinto EM, Billerbeck AE, Mendonca BB, Latronico AC. The unusually high incidence of germline Arg337His mutation in the p53 tumor suppressor gene among brazilian with adrenocortical tumors can be attributed to founder effect. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Vancouver
Pinto EM, Billerbeck AE, Mendonca BB, Latronico AC. The unusually high incidence of germline Arg337His mutation in the p53 tumor suppressor gene among brazilian with adrenocortical tumors can be attributed to founder effect. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Tall stature, absence of breast development and gonadal estrogen deficiency in a 45,X/46,X,der(X) patiente-overdosage of SHOX gene (2004)
Correa, R. V.; Nishi, M. Y.; Cruzes, A. L.; Carvalho, L. R. S.; Costa, E. M. F.; Mendonca, B. B.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: HORMÔNIOS SEXUAIS FEMININOS (ANORMALIDADES), CROMOSSOMOS SEXUAIS (ANORMALIDADES), SEQUENCIAMENTO GENÉTICO, ESTRÓGENOS
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ABNT
CORREA, R. V. et al. Tall stature, absence of breast development and gonadal estrogen deficiency in a 45,X/46,X,der(X) patiente-overdosage of SHOX gene. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 06 nov. 2025.
APA
Correa, R. V., Nishi, M. Y., Cruzes, A. L., Carvalho, L. R. S., Costa, E. M. F., & Mendonca, B. B. (2004). Tall stature, absence of breast development and gonadal estrogen deficiency in a 45,X/46,X,der(X) patiente-overdosage of SHOX gene. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Correa RV, Nishi MY, Cruzes AL, Carvalho LRS, Costa EMF, Mendonca BB. Tall stature, absence of breast development and gonadal estrogen deficiency in a 45,X/46,X,der(X) patiente-overdosage of SHOX gene. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Vancouver
Correa RV, Nishi MY, Cruzes AL, Carvalho LRS, Costa EMF, Mendonca BB. Tall stature, absence of breast development and gonadal estrogen deficiency in a 45,X/46,X,der(X) patiente-overdosage of SHOX gene. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
An improved method of DNA extraction by NaCl from oral cells obtained with a cytologic brush (2004)
Abrão, M.; Billerbeck, A.; Nishi, M.; Mendonca, B. B.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidades: FM, HU
Assuntos: DNA (EXTRAÇÃO;MÉTODOS), TÉCNICAS E PROCEDIMENTOS DE LABORATÓRIO (MÉTODOS), MUCOSA ORAL (FISIOPATOLOGIA), CÉLULAS
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ABNT
ABRÃO, M. et al. An improved method of DNA extraction by NaCl from oral cells obtained with a cytologic brush. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 06 nov. 2025.
APA
Abrão, M., Billerbeck, A., Nishi, M., & Mendonca, B. B. (2004). An improved method of DNA extraction by NaCl from oral cells obtained with a cytologic brush. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Abrão M, Billerbeck A, Nishi M, Mendonca BB. An improved method of DNA extraction by NaCl from oral cells obtained with a cytologic brush. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Vancouver
Abrão M, Billerbeck A, Nishi M, Mendonca BB. An improved method of DNA extraction by NaCl from oral cells obtained with a cytologic brush. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Diagnosis and treatment of girls with gonadotropin-independent precocious puberty due to automous ovarian cysts (2004)
d`Alva, C.; Latronico, A.; Brito, V.; Teles, M.; Arnhold, I.; Mendonca, B. B.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: PUBERDADE PRECOCE (ETIOLOGIA;GENÉTICA;DIAGNÓSTICO;TERAPIA), HORMÔNIOS SEXUAIS FEMININOS (GENÉTICA;ANORMALIDADES), CISTOS OVARIANOS (ETIOLOGIA)
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ABNT
D`ALVA, C. et al. Diagnosis and treatment of girls with gonadotropin-independent precocious puberty due to automous ovarian cysts. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 06 nov. 2025.
APA
d`Alva, C., Latronico, A., Brito, V., Teles, M., Arnhold, I., & Mendonca, B. B. (2004). Diagnosis and treatment of girls with gonadotropin-independent precocious puberty due to automous ovarian cysts. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
d`Alva C, Latronico A, Brito V, Teles M, Arnhold I, Mendonca BB. Diagnosis and treatment of girls with gonadotropin-independent precocious puberty due to automous ovarian cysts. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Vancouver
d`Alva C, Latronico A, Brito V, Teles M, Arnhold I, Mendonca BB. Diagnosis and treatment of girls with gonadotropin-independent precocious puberty due to automous ovarian cysts. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Final heigth in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency treated with cortisone acetate (2004)
Parente, E.; Marquezine, E.; Rodrigues, a.; Maureira, G.; Brenlha, E. M.; Ueti, R.; Arnhold, I.; Mendonca, B. B.; Bachega, T. A. S.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: CORTISOL (APLICAÇÕES TERAPÊUTICAS), HORMÔNIOS (DEFICIÊNCIA), TERAPIAS COMPLEMENTARES, HIPERPLASIA SUPRARRENAL CONGÊNITA
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ABNT
PARENTE, E. et al. Final heigth in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency treated with cortisone acetate. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 06 nov. 2025.
APA
Parente, E., Marquezine, E., Rodrigues, a., Maureira, G., Brenlha, E. M., Ueti, R., et al. (2004). Final heigth in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency treated with cortisone acetate. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Parente E, Marquezine E, Rodrigues a., Maureira G, Brenlha EM, Ueti R, Arnhold I, Mendonca BB, Bachega TAS. Final heigth in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency treated with cortisone acetate. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Vancouver
Parente E, Marquezine E, Rodrigues a., Maureira G, Brenlha EM, Ueti R, Arnhold I, Mendonca BB, Bachega TAS. Final heigth in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency treated with cortisone acetate. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Pattern of TSH and PRL response to TRH in patients presenting hypopituitarism with an identified hypothalamic or pituitary origin (2004)
Carvalho, L. R.; Berger, K.; Melo, M. E.; Abrao, M.; Nishi, M.; Marui, S.; Estefan, V.; Arnhold, I. J. P.; Mendonca, B. B.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: MUTAÇÃO GENÉTICA, GLÂNDULA PITUITÁRIA ANTERIOR (DEFICIÊNCIA), DIAGNÓSTICO DIFERENCIAL, HORMÔNIOS TIREOIDIANOS (DEFICIÊNCIA)
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ABNT
CARVALHO, L. R. et al. Pattern of TSH and PRL response to TRH in patients presenting hypopituitarism with an identified hypothalamic or pituitary origin. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 06 nov. 2025.
APA
Carvalho, L. R., Berger, K., Melo, M. E., Abrao, M., Nishi, M., Marui, S., et al. (2004). Pattern of TSH and PRL response to TRH in patients presenting hypopituitarism with an identified hypothalamic or pituitary origin. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Carvalho LR, Berger K, Melo ME, Abrao M, Nishi M, Marui S, Estefan V, Arnhold IJP, Mendonca BB. Pattern of TSH and PRL response to TRH in patients presenting hypopituitarism with an identified hypothalamic or pituitary origin. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Vancouver
Carvalho LR, Berger K, Melo ME, Abrao M, Nishi M, Marui S, Estefan V, Arnhold IJP, Mendonca BB. Pattern of TSH and PRL response to TRH in patients presenting hypopituitarism with an identified hypothalamic or pituitary origin. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Absence of FSHR activating mutations in women with iatrogenic ovarian hyperstimulation syndrome (2004)
d' Alva, C.; Serafini, P.; Motta, E.; Kohek, M.; Latronico, A.; Mendonca, B. B.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: FERTILIZAÇÃO "IN VITRO" (COMPLICAÇÕES), CISTOS OVARIANOS (COMPLICAÇÕES), OVULAÇÃO (TÉCNICAS), POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
D' ALVA, C. et al. Absence of FSHR activating mutations in women with iatrogenic ovarian hyperstimulation syndrome. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 06 nov. 2025.
APA
d' Alva, C., Serafini, P., Motta, E., Kohek, M., Latronico, A., & Mendonca, B. B. (2004). Absence of FSHR activating mutations in women with iatrogenic ovarian hyperstimulation syndrome. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
d' Alva C, Serafini P, Motta E, Kohek M, Latronico A, Mendonca BB. Absence of FSHR activating mutations in women with iatrogenic ovarian hyperstimulation syndrome. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Vancouver
d' Alva C, Serafini P, Motta E, Kohek M, Latronico A, Mendonca BB. Absence of FSHR activating mutations in women with iatrogenic ovarian hyperstimulation syndrome. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
A novel germiline mutation (6747_6748insG) of MEN1 Gene, in a patient with multiple endocrine neoplasia type 1 (2004)
Costa, M. H. S.; Domenice, S.; Pinto, E. M.; Martin, R. M.; Mimura, L. Y.; Mendonca, B. B.; Fragoso, M. C. B. V.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: NEOPLASIA ENDÓCRINA MÚLTIPLA, MUTAÇÃO GENÉTICA, TIREOIDECTOMIA, HIPERTIREOIDISMO (COMPLICAÇÕES), METÁSTASE (COMPLICAÇÕES)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COSTA, M. H. S. et al. A novel germiline mutation (6747_6748insG) of MEN1 Gene, in a patient with multiple endocrine neoplasia type 1. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 06 nov. 2025.
APA
Costa, M. H. S., Domenice, S., Pinto, E. M., Martin, R. M., Mimura, L. Y., Mendonca, B. B., & Fragoso, M. C. B. V. (2004). A novel germiline mutation (6747_6748insG) of MEN1 Gene, in a patient with multiple endocrine neoplasia type 1. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Costa MHS, Domenice S, Pinto EM, Martin RM, Mimura LY, Mendonca BB, Fragoso MCBV. A novel germiline mutation (6747_6748insG) of MEN1 Gene, in a patient with multiple endocrine neoplasia type 1. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Vancouver
Costa MHS, Domenice S, Pinto EM, Martin RM, Mimura LY, Mendonca BB, Fragoso MCBV. A novel germiline mutation (6747_6748insG) of MEN1 Gene, in a patient with multiple endocrine neoplasia type 1. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Treatment with cabergoline in teo cases of gonadotropin-producing pituitary ademaona: Dissociation between tumor growth inibition and control of ovarian hyperstimulation syndrome (2004)
Knoepfelmacher, M.; Danilovic, D.; Rosa, R; Mendonca, B. B.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: HORMÔNIOS HIPOFISÁRIOS (ANORMALIDADES), HORMÔNIOS SEXUAIS FEMININOS (ANORMALIDADES;TRATAMENTO), ADENOMA (ETIOLOGIA;CIRURGIA), IMUNOHISTOQUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KNOEPFELMACHER, M. et al. Treatment with cabergoline in teo cases of gonadotropin-producing pituitary ademaona: Dissociation between tumor growth inibition and control of ovarian hyperstimulation syndrome. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 06 nov. 2025.
APA
Knoepfelmacher, M., Danilovic, D., Rosa, R., & Mendonca, B. B. (2004). Treatment with cabergoline in teo cases of gonadotropin-producing pituitary ademaona: Dissociation between tumor growth inibition and control of ovarian hyperstimulation syndrome. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Knoepfelmacher M, Danilovic D, Rosa R, Mendonca BB. Treatment with cabergoline in teo cases of gonadotropin-producing pituitary ademaona: Dissociation between tumor growth inibition and control of ovarian hyperstimulation syndrome. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Vancouver
Knoepfelmacher M, Danilovic D, Rosa R, Mendonca BB. Treatment with cabergoline in teo cases of gonadotropin-producing pituitary ademaona: Dissociation between tumor growth inibition and control of ovarian hyperstimulation syndrome. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Analysis of the LHX4 gene in patients with hypopituitarism and ectopic posterior pituitary lobe: Identification of four novel allelic variations (2004)
Melo, M. E.; Marui, S.; Leite, C. C.; Mendonca, B. B.; knoepfelmacher, M.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: MUTAÇÃO GENÉTICA, GLÂNDULA PITUITÁRIA (ANORMALIDADES;DEFICIÊNCIA), SEQUENCIAMENTO GENÉTICO, HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MELO, M. E. et al. Analysis of the LHX4 gene in patients with hypopituitarism and ectopic posterior pituitary lobe: Identification of four novel allelic variations. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 06 nov. 2025.
APA
Melo, M. E., Marui, S., Leite, C. C., Mendonca, B. B., & knoepfelmacher, M. (2004). Analysis of the LHX4 gene in patients with hypopituitarism and ectopic posterior pituitary lobe: Identification of four novel allelic variations. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Melo ME, Marui S, Leite CC, Mendonca BB, knoepfelmacher M. Analysis of the LHX4 gene in patients with hypopituitarism and ectopic posterior pituitary lobe: Identification of four novel allelic variations. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Vancouver
Melo ME, Marui S, Leite CC, Mendonca BB, knoepfelmacher M. Analysis of the LHX4 gene in patients with hypopituitarism and ectopic posterior pituitary lobe: Identification of four novel allelic variations. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Study of CAG repeat in the exon 1 of the androgen receptor gene in 106 female patients with the classical form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency (2004)
Rocha, R.; Billerbeck, a. E.; Pinto, E.; Melo, K. F.; Lin, C. J.; Mendonca, B. B.; Bachega, T. A. S.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: HORMÔNIOS SEXUAIS FEMININOS (DEFICIÊNCIA), GENITÁLIA FEMININA (ANORMALIDADES), ATIVAÇÃO ENZIMÁTICA, RECEPTORES ANDROGÊNICOS (GENÉTICA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ROCHA, R. et al. Study of CAG repeat in the exon 1 of the androgen receptor gene in 106 female patients with the classical form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 06 nov. 2025.
APA
Rocha, R., Billerbeck, a. E., Pinto, E., Melo, K. F., Lin, C. J., Mendonca, B. B., & Bachega, T. A. S. (2004). Study of CAG repeat in the exon 1 of the androgen receptor gene in 106 female patients with the classical form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Rocha R, Billerbeck a. E, Pinto E, Melo KF, Lin CJ, Mendonca BB, Bachega TAS. Study of CAG repeat in the exon 1 of the androgen receptor gene in 106 female patients with the classical form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]
Vancouver
Rocha R, Billerbeck a. E, Pinto E, Melo KF, Lin CJ, Mendonca BB, Bachega TAS. Study of CAG repeat in the exon 1 of the androgen receptor gene in 106 female patients with the classical form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Program and Abstracts. 2004 ;[citado 2025 nov. 06 ]

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